esv3795750
- Organism: Homo sapiens
- Study:estd192 (COSMIC)
- Variant Type:complex chromosomal rearrangement
- Method Type:Curated
- Submitted on:GRCh37
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:2,001
- Description:
Chr4:g.(79908477_79910477)_chr6:(10422490_10424490)bkpt - Publication(s):Forbes et al. 2008, Forbes et al. 2008
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 98 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 101 SVs from 25 studies. See in: genome view
Overlapping variant regions from other studies: 98 SVs from 28 studies. See in: genome view
Overlapping variant regions from other studies: 101 SVs from 25 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| esv3795750 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 78,987,323 | 78,989,323 | 78,987,323 | 78,989,323 |
| esv3795750 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000006.12 | Chr6 | 10,422,257 | 10,424,257 | 10,422,257 | 10,424,257 |
| esv3795750 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 79,908,477 | 79,910,477 | 79,908,477 | 79,910,477 | ||
| esv3795750 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000006.11 | Chr6 | 10,422,490 | 10,424,490 | 10,422,490 | 10,424,490 |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Other Calls in this Sample and Study |
|---|---|---|---|---|---|
| essv16623332 | interchromosomal translocation | 2120208 | Curated | Curated | 66 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop | strand |
|---|---|---|---|---|---|---|---|---|---|---|---|
| essv16623332 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 78,987,323 | 78,989,323 | 78,987,323 | 78,989,323 | not reported |
| essv16623332 | Remapped | Perfect | GRCh38.p12 | First Pass | NC_000006.12 | Chr6 | 10,422,257 | 10,424,257 | 10,422,257 | 10,424,257 | not reported |
| essv16623332 | Submitted genomic | GRCh37 (hg19) | NC_000004.11 | Chr4 | 79,908,477 | 79,910,477 | 79,908,477 | 79,910,477 | not reported | ||
| essv16623332 | Submitted genomic | GRCh37 (hg19) | NC_000006.11 | Chr6 | 10,422,490 | 10,424,490 | 10,422,490 | 10,424,490 | not reported |